Reconstruction of an excited-state molecular wave packet with attosecond transient absorption spectroscopy

Attosecond science promises to allow new forms of quantum control in which a broadband isolated attosecond pulse excites a molecular wave packet consisting of a coherent superposition of multiple excited electronic states. This electronic excitation triggers nuclear motion on the molecular manifold...

Descripción completa

Detalles Bibliográficos
Autores: Cheng, Yan, Chini, Michael, Wang, Xiaowei, Gonzalez-Castrillo, Alberto, Palacios Cañas, Alicia, Argenti, Luca, Martín García, Fernando, Chang, Zenghu
Tipo de recurso: artículo
Fecha de publicación:2016
País:España
Institución:Universidad Autónoma de Madrid
Repositorio:Biblos-e Archivo. Repositorio Institucional de la UAM
Idioma:inglés
OAI Identifier:oai:repositorio.uam.es:10486/677681
Acceso en línea:http://hdl.handle.net/10486/677681
https://dx.doi.org/10.1103/PhysRevA.94.023403
Access Level:acceso abierto
Palabra clave:Molecular wave
Attosecond
Absorption spectroscopy
Química
Descripción
Sumario:Attosecond science promises to allow new forms of quantum control in which a broadband isolated attosecond pulse excites a molecular wave packet consisting of a coherent superposition of multiple excited electronic states. This electronic excitation triggers nuclear motion on the molecular manifold of potential energy surfaces and can result in permanent rearrangement of the constituent atoms. Here, we demonstrate attosecond transient absorption spectroscopy (ATAS) as a viable probe of the electronic and nuclear dynamics initiated in excited states of a neutral molecule by a broadband vacuum ultraviolet pulse. Owing to the high spectral and temporal resolution of ATAS, we are able to reconstruct the time evolution of a vibrational wave packet within the excited B′Σu1+ electronic state of H2 via the laser-perturbed transient absorption spectrum